Glycerides are fatty acid esters of glycerol; they are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils. 99769-19-4, formula is C8H9BO4, Name is 3-(Methoxycarbonyl)phenylboronic acid. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Name: 3-(Methoxycarbonyl)phenylboronic acid.
Chen, Xiao-Bing;Li, Li;Yang, Wan-Chun;Song, Kun-Long;Wu, Bin;Gan, Wan-Er;Cao, Jian;Xu, Li-Wen research published 《 Palladium-Catalyzed C-C Bond Activation/Suzuki Reaction of Methylenecyclobutanes》, the research content is summarized as follows. A novel palladium-catalyzed C-C bond activation manner of methylenecyclobutanes followed by subsequent Suzuki cross-coupling reaction afforded multisubstituted indanes. The tandem reaction process involved intramol. carbopalladation of double bond, β-carbon elimination and intermol. trapping of the transient σ-alkylpalladium complex with boronic acids. A new TADDOL-derived phosphoramidite ligand bearing fluorine and silicon-based bulky groups was found to be efficient for C-C bond activation of methylenecyclobutanes.
99769-19-4, 3-Methoxycarbonylphenylboronic acid is a useful research compound. Its molecular formula is C8H9BO4 and its molecular weight is 179.97 g/mol. The purity is usually 95%.
3-Methoxycarbonylphenylboronic acid is a reactanct that has been involved in a variety of applications. For instance, it has been used in Suzuki-Miyaura cross-coupling, Iterative cross-coupling of boronate building blocks, cross-coupling with aryl/ alkenyl sulfonates, synthesis of symmetrical biaryls via CuCl catalyzed homocoupling, trifluoromethylation, and cyanation just to name a few of its many uses.
3-Methoxycarbonylphenylboronic acid is a boronate ligand that has been shown to have an interaction with the nitrogen atoms in amines. This compound is used for the Suzuki coupling reaction, which is a chemical reaction between an organoboron compound and an organic electrophile. 3-Methoxycarbonylphenylboronic acid has a helical structure that can be seen by FTIR spectroscopy and it has potent inhibitory activity., Name: 3-(Methoxycarbonyl)phenylboronic acid
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